一个不寻常的中央巨细胞肉芽肿病例

IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE Journal of Oral and Maxillofacial Surgery Medicine and Pathology Pub Date : 2024-05-05 DOI:10.1016/j.ajoms.2024.04.018
Yap Boon How , Ajay Telang , Lahari Telang , Wanninayake Mudiyanselage Tilakaratne
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引用次数: 0

摘要

导言颌骨中央巨细胞肉芽肿(CGCG)具有特征性诊断特征。但在极少数情况下,它们可能表现出略微不同的特征或与其他病变相关的特征。病例报告 我们报告了一名 47 岁男性患者的颌骨病变,患者表现为左下颌骨弥漫性肿胀,疼痛异常。虽然二维成像检查显示为囊性病变,但三维成像检查显示病变的分界更加清晰。详细检查后,病变完全切除,组织病理学诊断为 CGCG。结论诊断由显示两种或两种以上不同特征的区域组成的颌骨病变总是具有挑战性。本报告强调了组织病理学的主要发现,这些发现有助于区分混合型病变和具有大面积反应性骨区的 CGCG 病例。
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An unusual case of Central Giant Cell Granuloma

Introduction

Central Giant Cell Granuloma (CGCG) in jaw bones have characteristic diagnostic features. But rarely they may present with slightly different features or features related to other lesions. It can be challenging when histopathological features of two or more different entities are seen within a single lesion.

Case report

We report a jaw lesion in a 47-year-old male patient who presented unusually as a painful diffuse left mandibular swelling. Although the 2-dimensional imaging study suggested a cystic lesion, the 3-dimensional imaging study pointed to a more well-demarcated pathology. A complete excision of the lesion when examined in detail confirmed a histopathologic diagnosis of a CGCG. The challenge however was the large reactive bone areas that raised a suspicion of an Ossifying Fibroma lesion.

Conclusion

Diagnosing a jaw lesion consisting of areas showing two or more different features is always challenging. This report highlights the key histopathologic findings that can help distinguish between a hybrid lesion and a case of CGCG with large reactive bone areas.
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来源期刊
CiteScore
0.80
自引率
0.00%
发文量
129
审稿时长
83 days
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